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Unit 4 Drug Stability
Unit 4 Drug Stability

... Drug Stability Steps to prevent instability Design of product based on proper pre-formulation studies. ...
formulation and evaluation of irbesartan
formulation and evaluation of irbesartan

... within the limit and hence all formulation passes the weight variation test. The drug content was found to be uniform among all formulation and ranged from 69.50% to 99.50%. The hardness of tablets of all formulations was from 100 to 145N. The friability of tablets of all formulations ranged from 0. ...
Formulation Strategies for `First-Into-Man` Studies
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... alter their overall therapeutic profile. In favourable cases, this modification has the potential to have a positive impact effect on safety, efficacy and/or tolerability. By starting from compounds with welldefined human pharmacological effects – such as approved drugs – deuteration potentially pro ...
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Pharmacology of Airway Management

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The Development of Deuterium-Containing Drugs
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cost effective analysis of commonly used topical drugs in

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... and death. Other sedatives that have no known medical use in the United States, such as GHB, Rohypnol (Roofies), and methaqualone (Quaaludes) are also drugs of high value and interest on the black market. These drugs produce an intoxicating effect similar to alcohol and can even cause loss of motor ...
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A study of adverse drug reactions due to antihypertensive drugs in a

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เภสัชจลนศาสตร์

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studies on formulation and evaluation of floating tablet
studies on formulation and evaluation of floating tablet

... approximately 85% with little intersubject variations. The serum concentration reaches its peak (c) within 1-2 hrs after oral administration.3 Oral delivery of drugs is by far the most preferable route of drug delivery due to the ease of administration, low cost of therapy, patient compliance and fl ...
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Orphan drug

An orphan drug is a pharmaceutical agent that has been developed specifically to treat a rare medical condition, the condition itself being referred to as an orphan disease.In the US and EU it is easier to gain marketing approval for an orphan drug, and there may be other financial incentives, such as extended exclusivity periods, all intended to encourage the development of drugs which might otherwise lack a sufficient profit motive. The assignment of orphan status to a disease and to any drugs developed to treat it is a matter of public policy in many countries, and has resulted in medical breakthroughs that may not have otherwise been achieved due to the economics of drug research and development.According to Thomson Reuters in their 2012 publication ""The Economic Power of Orphan Drugs"", there has been increased investing in orphan drug Research and Development partly due to the U. S. Orphan Drug Act (ODA) 1983 and similar Acts in other regions of the world and also driven by ""high-profile philanthropic funding."" The period between 2001 to 2011 was the ""most productive period in the history of orphan drug development, in terms of average annual orphan drug designations and orphan drug approvals."" For the same decade the compound annual growth rate (CAGR) of the orphan drugs was an ""impressive 25.8 percent, compared to only 20.1 percent for a matched control group of non-orphan drugs."" By 2012 the market for orphan drugs was worth USD$637 million compared to the USD$638 million matched control group of non-orphan drugs, Thomson Reuters.By 2012, ""the revenue-generating potential of orphan drugs [was] as great as for non-orphan drugs, even though patient populations for rare diseases are significantly smaller. Moreover, we suggest that orphan drugs have greater profitability when considered in the full context of developmental drivers including government financial incentives, smaller clinical trial sizes, shorter clinical trial times and higher rates of regulatory success.""
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